Canonical Allele Identifier: CA1619467752
Gene: NOTCH4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.32202722_32202726delinsCAGAG , CM000668.2:g.32202722_32202726delinsCAGAG GRCh38
NC_000006.11:g.32170499_32170503delinsCAGAG , CM000668.1:g.32170499_32170503delinsCAGAG GRCh37
NC_000006.10:g.32278477_32278481delinsCAGAG NCBI36
NG_028190.1:g.26342_26346delinsCTCTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000375023.3:c.3232-127_3232-123delinsCTCTG MANE Select ENSP00000364163.3:n.3232-127_3232-123delinsCTCTG
ENST00000474612.1:n.1191_1195delinsCTCTG
NM_004557.3:c.3232-127_3232-123delinsCTCTG NP_004548.3:n.3232-127_3232-123delinsCTCTG
NR_134949.1:n.3472+1044_3472+1048delinsCTCTG
NR_134950.1:n.3370+1044_3370+1048delinsCTCTG
NM_004557.4:c.3232-127_3232-123delinsCTCTG MANE Select NP_004548.3:n.3232-127_3232-123delinsCTCTG
NR_134949.2:n.3472+1044_3472+1048delinsCTCTG
NR_134950.2:n.3370+1044_3370+1048delinsCTCTG